Harraghy Niamh, Kormanec Jan, Wolz Christiane, Homerova Dagmar, Goerke Christiane, Ohlsen Knut, Qazi Saara, Hill Philip, Herrmann Mathias
Institute of Medical Microbiology and Hygiene, Building 43, University of Saarland, D-66421 Homburg/Saar, Germany.
Institute of Molecular Biology, Center of Excellence for Molecular Medicine, Slovak Academy of Sciences, 845 51 Bratislava, Slovak Republic.
Microbiology (Reading). 2005 Jun;151(Pt 6):1789-1800. doi: 10.1099/mic.0.27902-0.
Eap and Emp are two Staphylococcus aureus adhesins initially described as extracellular matrix binding proteins. Eap has since emerged as being important in adherence to and invasion of eukaryotic cells, as well as being described as an immunomodulator and virulence factor in chronic infections. This paper describes the mapping of the transcription start point of the eap and emp promoters. Moreover, using reporter-gene assays and real-time PCR in defined regulatory mutants, environmental conditions and global regulators affecting expression of eap and emp were investigated. Marked differences were found in expression of eap and emp between strain Newman and the 8325 derivatives SH1000 and 8325-4. Moreover, both genes were repressed in the presence of glucose. Analysis of expression of both genes in various regulatory mutants revealed that sarA and agr were involved in their regulation, but the data suggested that there were additional regulators of both genes. In a sae mutant, expression of both genes was severely repressed. sae expression was also reduced in the presence of glucose, suggesting that repression of eap and emp in glucose-containing medium may, in part, be a consequence of a decrease in expression of sae.
Eap和Emp是两种最初被描述为细胞外基质结合蛋白的金黄色葡萄球菌黏附素。此后,Eap已被证明在黏附并侵入真核细胞方面很重要,并且在慢性感染中被描述为一种免疫调节剂和毒力因子。本文描述了eap和emp启动子转录起始点的定位。此外,利用报告基因检测和在特定调控突变体中的实时PCR,研究了影响eap和emp表达的环境条件和全局调控因子。发现纽曼菌株与8325衍生物SH1000和8325 - 4之间eap和emp的表达存在显著差异。此外,在葡萄糖存在的情况下,这两个基因均受到抑制。对各种调控突变体中这两个基因表达的分析表明,sarA和agr参与了它们的调控,但数据表明这两个基因还有其他调控因子。在sae突变体中,这两个基因的表达均受到严重抑制。在葡萄糖存在的情况下,sae的表达也降低,这表明在含葡萄糖的培养基中eap和emp的抑制可能部分是sae表达降低的结果。